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Chemische Prozesse und Phasenübergänge Poster: Mi., 14:00–16:30 M-P168<br />

Surface oxidation of metals using oxygen ion beams<br />

Nikolai Alov 1<br />

1 Lomonosov Moscow State University, 119992 Moscow, Russia<br />

Surface oxidation of Mo, W, Nb and Ta using oxygen ion beams was investigated by Xray<br />

photoelectron spectroscopy (XPS). Irradiation by oxygen ion beams was carried out<br />

at room temperature with ion energy of 1-5 keV, dose of 10 15 -10 18 cm −2 and direction<br />

normal to surface. XPS analysis of oxidized metal surfaces was performed in situ using<br />

Leybold LHS-10 electron spectrometer. The fitted XPS spectra of Mo 3d and W 4f core<br />

levels show that the metal oxidation states 4+, 5+ and 6+ are present in oxide films.<br />

At the initial stage of irradiation the rapid oxidation of Mo and W surface layers was<br />

observed. At higher dose, which depends on the energy of oxygen ions and the kind of<br />

metal, the oxidation of surface layers reaches saturation and the surface composition<br />

remains almost unchanged with increasing irradiation dose. The fitted XPS spectra<br />

of Nb 3d and Ta 4f core levels show that the metal oxidation states 2+, 4+ and 5+<br />

are present in oxide films. At the initial stage of irradiation the rapid oxidation of Nb<br />

and Ta surface layers was observed. However, at higher dose, which depends on the<br />

energy of oxygen ions and the kind of metal, the population of Nb2+, Nb4+, Ta2+ and<br />

Ta4+ reaches a maximum and then begins to decrease. The population of Nb5+ and<br />

Ta5+ continues to increase and the entire oxide films will consist of only Nb5+ and<br />

Ta5+. Using XPS data the absolute values of fundamental parameters of low-energy<br />

oxygen ion interaction with metal surfaces (reaction and sputtering cross-sections) were<br />

calculated.

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